Nathalie Neyroud

Paris, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

Software-based analysis of T-wave morphology: identifying the electrocardiogram signature of high-risk long QT syndrome.

Software-based analysis of T-wave morphology: identifying the electrocardiogram signature of high-risk long QT syndrome.

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

Published: May 30, 2025

Systematic analysis of SCN5A variants associated with inherited cardiac diseases.

Systematic analysis of SCN5A variants associated with inherited cardiac diseases.

Journal: Heart rhythm

Published: June 06, 2024

Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients.

Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients.

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

Published: March 05, 2024

Editorial: Methods and applications in cardiac electrophysiology-application to inherited arrhythmias.

Editorial: Methods and applications in cardiac electrophysiology-application to inherited arrhythmias.

Journal: Frontiers in physiology

Published: February 19, 2024

Intracardiac electrophysiology to characterize susceptibility to ventricular arrhythmias in murine models.

Intracardiac electrophysiology to characterize susceptibility to ventricular arrhythmias in murine models.

Journal: Frontiers in physiology

Published: October 23, 2023

Trafficking and Gating Cooperation Between Deficient Nav1.5-mutant Channels to Rescue INa.

Trafficking and Gating Cooperation Between Deficient Nav1.5-mutant Channels to Rescue INa.

Journal: Frontiers in bioscience (Landmark edition)

Published: January 07, 2022

Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition.

Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition.

Journal: Stem cell research

Published: December 03, 2021

A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response.

A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response.

Journal: Journal of personalized medicine

Published: May 06, 2021

In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant.

In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant.

Journal: Frontiers in physiology

Published: January 30, 2021

Inter-Regulation of Kv4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies.

Inter-Regulation of Kv4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies.

Journal: International journal of molecular sciences

Published: June 10, 2020

A novel gain-of-function mutation in SCN5A responsible for multifocal ectopic Purkinje-related premature contractions.

A novel gain-of-function mutation in SCN5A responsible for multifocal ectopic Purkinje-related premature contractions.

Journal: Human mutation

Published: July 23, 2019

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation.

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation.

Journal: Heart rhythm

Published: November 08, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026